Supervise day-to-day maintenance and troubleshooting of production equipment and utilities. Ensure preventive and breakdown maintenance is carried out as per schedule. Monitor the performance of equipment used in Granulation, Compression, C...

"• Operation, & Maintenance, of all packaging equipment & Parenteral of following block: Main Pharma Block. Cephalosporin Block, Rifampicin Block • Operation & Maintenance of associated systems • To develop Total Quality Maintenance system ...

Job Purpose & Core Mandate The Manufacturing Excellence Leader is globally responsible for driving operational efficiency, cost optimization, and business transformation across all Formulation and API manufacturing facilities. This corporat...

"• To ensure compliance of cGMP requirements & Good Engineering Practices, other statutory laws, rules and regulations. • Planning of work and manpower on day to day basis. • Ensure efficient operation and maintenance of HVAC system. • To e...

To co-ordinate the GMP audits on the site, Audit Checklist execution, follow up for the CAPA, preparation of compliance report and to ensure the effective implementation of CAPA • To conduct monthly Quality Review Meeting and follow-up the ...

Role Objective / Major Purpose of the Job To lead and manage all operations of the Cephalosporin Department, ensuring timely completion of packaging activities in compliance with current Good Manufacturing Practices (cGMP), Schedule M, appr...

1) Assist in preventive, predictive, and breakdown maintenance of manufacturing equipment. 2) Support maintenance of equipment such as mixers, granulators, compression machines, coating machines, filling machines, pumps, and packaging equip...

Planning and Execution of all MMD-I & BPR preparation activity pertaining to Main Pharma Block, Cephalosporin Block, Penicillin Block & Rifampicin Block of Dholka, as well as Contract Manufacturing & Herbal. • Preparation and review of MMD-...

To manage the P2P purchase team to ensure procurement of required goods at the right price, right quality and right time • To manage the Gift purchase team to ensure procurement of required goods at the right price, right quality and right ...

Principal task and Responsibilities: -Supervising & performing production activities of Streptokinase Drug Substance -Troubleshoot the technical issues in consultation with the Production Head during the shift duties. -Participate in audits...

"• To prepare and maintain SOP and documents related to Plant preventive maintenance. • To conduct routine breakdown maintenance of Main Pharma Block equipment’s. • To follow and implement PPM schedule for effective implementation in shorte...

Plan and execute preventive, predictive, and breakdown maintenance activities. Ensure maximum equipment availability and minimize production downtime. Troubleshoot mechanical, electrical, and utility-related failures. Maintain maintenance r...

Ensure smooth operation of HVAC systems, AHUs, chillers, boilers, cooling towers, compressors, and other plant utilities. Monitor purified water (PW), water for injection (WFI), and purified water generation/distribution systems, where appl...

"• Ensure efficient operation and maintenance of Utility (Boiler, chilling plant, Air compressor, cooling tower and N2 System). • To ensure strict compliance of cGMP requirements & Good Engineering Practice requirements besides other statut...

To ensure compliance of cGMP requirements & Good Engineering Practices, other statutory laws, rules and regulations. • Planning of work and manpower on day to day basis. • Ensure efficient operation and maintenance of HVAC system. • To ensu...

Plan and execute preventive, predictive, and breakdown maintenance activities. Ensure maximum equipment availability and minimize production downtime. Troubleshoot mechanical, electrical, and utility-related failures. Maintain maintenance r...

Follow cGMP and GLP practices in quality control lab. • To prepare Specification Master as per STP in SAP/LIMS. • To follow safety Procedure in QC department. • Preparation of COA as per current specification for Packing samples (whenever r...

"• To comply cGMP requirements & Good Engineering Practice requirements besides other statutory laws, rules and regulations. • To conduct routine break down maintenance of R&D and Bio-tech section equipment’s. • To follow and implement PPM ...

"Major Purpose of the Job: -To develop cost effective and robust process of API. Principal Tasks and Responsibilities: -To develop chemical process which is having least hazardous chemicals and cost effective process of API in lab and the t...

To perform In-process Quality Assurance for the process / products being manufactured and packed in Main Pharma Block (Tablet / Capsule). To ensure Quality and cGMP compliance of the products being manufactured and Packed in Main Pharma Blo...